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Vadim Y. Dudkin, Ph.D. - Publications

Affiliations: 
2001 University of Illinois at Chicago, Chicago, IL, United States 
Area:
diastereoselective free radical chemistry, acyl radical chemistry, enantioselective synthesis of á-disubstituted amino acids, and carbohydrate chemistry
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14 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2010 Caulfield MJ, Dudkin VY, Ottinger EA, Getty KL, Zuck PD, Kaufhold RM, Hepler RW, McGaughey GB, Citron M, Hrin RC, Wang YJ, Miller MD, Joyce JG. Small molecule mimetics of an HIV-1 gp41 fusion intermediate as vaccine leads. The Journal of Biological Chemistry. 285: 40604-11. PMID 20943652 DOI: 10.1074/Jbc.M110.172197  0.332
2010 Crich D, Dudkin V. ChemInform Abstract: Why Are the Hydroxy Groups of Partially Protected N-Acetylglucosamine Derivatives Such Poor Glycosyl Acceptors, and What Can Be Done about It? A Comparative Study of the Reactivity of N-Acetyl-, N-Phthalimido-, and 2-azido-2-deoxy-glu Cheminform. 32: no-no. DOI: 10.1002/chin.200143218  0.438
2008 Joyce JG, Krauss IJ, Song HC, Opalka DW, Grimm KM, Nahas DD, Esser MT, Hrin R, Feng M, Dudkin VY, Chastain M, Shiver JW, Danishefsky SJ. An oligosaccharide-based HIV-1 2G12 mimotope vaccine induces carbohydrate-specific antibodies that fail to neutralize HIV-1 virions. Proceedings of the National Academy of Sciences of the United States of America. 105: 15684-9. PMID 18838688 DOI: 10.1073/Pnas.0807837105  0.327
2007 de Jong A, Arce EC, Cheng TY, van Summeren RP, Feringa BL, Dudkin V, Crich D, Matsunaga I, Minnaard AJ, Moody DB. CD1c presentation of synthetic glycolipid antigens with foreign alkyl branching motifs. Chemistry & Biology. 14: 1232-42. PMID 18022562 DOI: 10.1016/J.Chembiol.2007.09.010  0.336
2007 Krauss IJ, Joyce JG, Finnefrock AC, Song HC, Dudkin VY, Geng X, Warren JD, Chastain M, Shiver JW, Danishefsky SJ. Fully synthetic carbohydrate HIV antigens designed on the logic of the 2G12 antibody. Journal of the American Chemical Society. 129: 11042-4. PMID 17711286 DOI: 10.1021/Ja074804R  0.302
2006 Wang ZG, Warren JD, Dudkin VY, Zhang X, Iserloh U, Visser M, Eckhardt M, Seeberger PH, Danishefsky SJ. A highly convergent synthesis of an N-linked glycopeptide presenting the H-type 2 human blood group determinant Tetrahedron. 62: 4954-4978. DOI: 10.1016/J.Tet.2006.02.080  0.346
2004 Dudkin VY, Orlova M, Geng X, Mandal M, Olson WC, Danishefsky SJ. Toward fully synthetic carbohydrate-based HIV antigen design: on the critical role of bivalency. Journal of the American Chemical Society. 126: 9560-2. PMID 15291558 DOI: 10.1021/Ja047720G  0.314
2004 Geng X, Dudkin VY, Mandal M, Danishefsky SJ. In pursuit of carbohydrate-based HIV vaccines, part 2: The total synthesis of high-mannose-type gp120 fragments--evaluation of strategies directed to maximal convergence. Angewandte Chemie (International Ed. in English). 43: 2562-5. PMID 15127453 DOI: 10.1002/Anie.200353626  0.302
2004 Dudkin VY, Miller JS, Danishefsky SJ. Chemical synthesis of normal and transformed PSA glycopeptides. Journal of the American Chemical Society. 126: 736-8. PMID 14733546 DOI: 10.1021/Ja037988S  0.357
2003 Dudkin VY, Crich D. A short synthesis of the trisaccharide building block of the N-linked glycans Tetrahedron Letters. 44: 1787-1789. DOI: 10.1016/S0040-4039(03)00102-3  0.483
2003 Dudkin VY, Miller JS, Danishefsky SJ. A concise route to the core pentasaccharide of N-linked glycoproteins Tetrahedron Letters. 44: 1791-1793. DOI: 10.1016/S0040-4039(03)00101-1  0.413
2002 Crich D, Dudkin V. Confirmation of the connectivity of 4,8,12,16,20-pentamethylpentacosylphoshoryl β-D-mannopyranoside, an unusual β-mannosyl phosphoisoprenoid from Mycobacterium avium, through synthesis Journal of the American Chemical Society. 124: 2263-2266. PMID 11878980 DOI: 10.1021/Ja0123958  0.404
2001 Crich D, Dudkin V. Why are the hydroxy groups of partially protected N-acetylglucosamine derivatives such poor glycosyl acceptors, and what can be done about it? A comparative study of the reactivity of N-acetyl-, N-phthalimido-, and 2-azido-2-deoxy-glucosamine derivatives in glycosylation. 2-Picolinyl ethers as reactivity-enhancing replacements for benzyl ethers Journal of the American Chemical Society. 123: 6819-6825. PMID 11448186 DOI: 10.1021/Ja010086B  0.45
2000 Crich D, Dudkin V. An unusual example of steric buttressing in glycosylation Tetrahedron Letters. 41: 5643-5646. DOI: 10.1016/S0040-4039(00)00941-2  0.339
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